A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527599



Internal ID15454892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24591626..24708291hg38UCSC Ensembl
Innerchr7:24631245..24747910hg19UCSC Ensembl
Innerchr7:24597770..24714435hg18UCSC Ensembl
Innerchr7:24404485..24521150hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38116666
hg19116666
hg18116666
hg17116666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704061
Samples
Known GenesDFNA5, MPP6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527599
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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